Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.853329G>A , CM000681.2:g.853329G>A | GRCh38 |
| NC_000019.9:g.853329G>A , CM000681.1:g.853329G>A | GRCh37 |
| NC_000019.8:g.804329G>A | NCBI36 |
| NG_009627.1:g.6039G>A , LRG_57:g.6039G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001972.4:c.292G>A MANE Select | NP_001963.1:p.Val98Met |
| ENST00000263621.2:c.292G>A MANE Select | ENSP00000263621.1:p.Val98Met |
| NM_001972.2:c.292G>A , LRG_57t1:c.292G>A | NP_001963.1:p.Val98Met |
| NM_001972.3:c.292G>A | NP_001963.1:p.Val98Met |
| ENST00000263621.1:c.292G>A | ENSP00000263621.1:p.Val98Met |
| ENST00000590230.5:c.292G>A | ENSP00000466090.1:p.Val98Met |
| XM_011527775.1:c.292G>A | XP_011526077.1:p.Val98Met |
| XM_011527776.1:c.292G>A | XP_011526078.1:p.Val98Met |